NDC 72835-302 Podiatrole
Ketoconazole 2% And Urea 20% Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
Code Structure Chart
Product Details
What is NDC 72835-302?
What are the uses for Podiatrole?
Which are Podiatrole UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOCONAZOLE (UNII: R9400W927I)
- KETOCONAZOLE (UNII: R9400W927I) (Active Moiety)
- UREA (UNII: 8W8T17847W)
- UREA (UNII: 8W8T17847W) (Active Moiety)
Which are Podiatrole Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Podiatrole?
- RxCUI: 198886 - urea 20 % Topical Cream
- RxCUI: 198886 - urea 200 MG/ML Topical Cream
- RxCUI: 198886 - urea 17 GM in 85 GM Topical Cream
- RxCUI: 203088 - ketoconazole 2 % Topical Cream
- RxCUI: 203088 - ketoconazole 20 MG/ML Topical Cream
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".